Phase 3 Lymphoma Trial, Recruiting NCT04834024 Sponsor: Beijing Mabworks Biotech Co., Ltd. Condition: Lymphoma
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Phase 3 Lymphoma Trial, Recruiting

NCT04834024
Recruiting Phase 3

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older
  • People who have been diagnosed with a type of slow-growing blood cancer called follicular lymphoma (FL), confirmed by a tissue sample, that is classified as Grade 1, 2, or 3a, and tests positive for a marker called CD20
  • People whose cancer has stopped responding to a treatment called rituximab
  • People who are generally well enough to carry out daily activities, rated on a standard medical scale as 0, 1, or 2 (meaning fully active to capable of light work)
  • People who have at least one measurable area of cancer visible on a CT scan, meeting specific size requirements
  • People with adequate blood cell and organ function levels
  • People with a life expectancy greater than 5 years
  • People who are willing and able to give written consent and follow the study requirements

Who may not be able to join:

  • People whose cancer has already stopped responding to a drug called lenalidomide
  • People whose lymphoma has spread to the brain or spinal cord
  • People with a serious brain condition called progressive multifocal leukoencephalopathy (PML)
  • People who have received certain antibody-based treatments (other than rituximab) within the 3 months before the study starts
  • People who have previously received any cancer vaccine
  • People who have had radiation therapy within 42 days before joining the study
  • People who have had chemotherapy within 28 days before joining the study
  • People with a history of another cancer in the last 3 years, except for certain fully treated skin cancers or a specific low-grade cervical condition
  • People who have had severe allergic reactions to antibody-based treatments in the past
  • People with a known allergy or sensitivity to the drugs thalidomide or lenalidomide
  • People who have been regularly taking steroid medications before the start of the trial, unless the steroids are being used for a reason unrelated to lymphoma and at a low dose (confirm with trial site)
  • People with serious heart conditions, such as certain types of heart failure, recent heart attack within the last 6 months, or unstable heart rhythms, or serious lung conditions such as obstructive pulmonary disease or a history of airway spasms
  • People who have HIV, hepatitis B, or hepatitis C infection (including specific markers detected on blood tests)
  • People who are pregnant or breastfeeding

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 8610-87788293

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Beijing Mabworks Biotech Co., Ltd.
Registry
ClinicalTrials.gov
Start date
2 June 2021
Est. completion
1 March 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-free Survival (per IRC)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov